AI Article Synopsis

  • Drug-induced liver injury in children (cDILI) is rare, making up about 1% of all adverse drug reactions and a significant portion of acute liver failure cases in kids, but studies show that their susceptibility might be more drug-specific than previously assumed.
  • Certain drugs, such as valproic acid and dactinomycin, are more likely to cause cDILI, while others, like deferasirox and isoniazid, are associated with liver injury in adults (aDILI) instead.
  • There is a critical knowledge gap in understanding the differences in how children and adults react to liver injuries caused by medication, as current animal models and diagnostic tools are lacking.

Article Abstract

Drug-induced liver injury in children (cDILI) accounts for about 1% of all reported adverse drug reactions throughout all age groups, less than 10% of all clinical DILI cases, and around 20% of all acute liver failure cases in children. The overall DILI susceptibility in children has been assumed to be lower than in adults. Nevertheless, controversial evidence is emerging about children's sensitivity to DILI, with children's relative susceptibility to DILI appearing to be highly drug-specific. The culprit drugs in cDILI are similar but not identical to DILI in adults (aDILI). This is demonstrated by recent findings that a drug frequently associated with aDILI (amoxicillin/clavulanate) was rarely associated with cDILI and that the drug basiliximab caused only cDILI but not aDILI. The fatality in reported cDILI studies ranged from 4% to 31%. According to the US Food and Drug Administration-approved drugs labels, valproic acid, dactinomycin, and ampicillin appear more likely to cause cDILI. In contrast, deferasirox, isoniazid, dantrolene, and levofloxacin appear more likely to cause aDILI. Animal models have been explored to mimic children's increased susceptibility to valproic acid hepatotoxicity or decreased susceptibility to acetaminophen or halothane hepatotoxicity. However, for most drugs, animal models are not readily available, and the underlying mechanisms for the differential reactions to DILI between children and adults remain highly hypothetical. Diagnosis tools for cDILI are not yet available. A critical need exists to fill the knowledge gaps in cDILI. This review article provides an overview of cDILI and specific drugs associated with cDILI.

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http://dx.doi.org/10.1177/1091581817721675DOI Listing

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